Pulmonary hypertension in newborns, also known as neonatal pulmonary hypertension, is a serious and potentially life-threatening condition characterized by high blood pressure in the lungs’ arteries. This condition can significantly impact the oxygenation of the newborn’s body, leading to critical health issues. Recent advancements in genetic research have identified a connection between the CRHR1 gene […]
Understanding MT-TL1 Gene MELAS Syndrome Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes, commonly known as MELAS syndrome, is a rare genetic disorder that affects multiple systems in the body, including the brain and muscles. It is primarily caused by mutations in the mitochondrial DNA, particularly in the MT-TL1 gene. Understanding the symptoms associated with […]
“` Symptoms of EIF2AK4 Gene Pulmonary Venoocclusive Disease Type 2 Genetic Test Pulmonary Venoocclusive Disease Type 2 (PVOD2) is a rare and severe form of pulmonary hypertension that affects the small veins in the lungs. It is caused by mutations in the EIF2AK4 gene. Understanding the symptoms of this condition is crucial for early diagnosis […]
Symptoms of SNTA1 Gene Long QT Syndrome Type 12 Long QT Syndrome Type 12, associated with mutations in the SNTA1 gene, is a rare inherited condition that can lead to serious heart rhythm abnormalities. It is crucial for individuals to be aware of the symptoms associated with this condition to seek timely medical intervention. The […]
DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a comprehensive range of services designed to provide individuals with vital health information. Among its extensive portfolio of genetic tests, the KCNJ5 Gene Long QT Syndrome Type 13 Genetic Test stands out as a critical tool for diagnosing this rare but serious […]
Symptoms of CALM2 Gene Long QT Syndrome Type 15 Long QT Syndrome (LQTS) is a disorder of the heart’s electrical activity. It can cause sudden, uncontrollable, and dangerous arrhythmias in response to exercise or stress. Type 15, specifically linked to mutations in the CALM2 gene, is a rare but significant variant of this condition. Recognizing […]
Long QT Syndrome (LQTS) is a rare inherited heart condition that can lead to serious or even life-threatening arrhythmias. Among the several genes associated with LQTS, the KCNH2 gene is notable for its role in Long QT Syndrome type 2 (LQT2). Understanding the symptoms associated with LQT2 and the importance of genetic testing is crucial […]
Long QT Syndrome (LQTS) is a disorder of the heart’s electrical activity that can lead to sudden and uncontrollable arrhythmias. Among the various types of LQTS, Type 3, linked to mutations in the SCN5A gene, is particularly significant due to its unique characteristics and implications for affected individuals. DNA Labs UAE offers a comprehensive genetic […]
Long QT syndrome (LQTS) is a rare heart condition that can potentially lead to life-threatening arrhythmias. Among the various types of LQTS, type 4, also known as Andersen-Tawil syndrome, is associated with mutations in the ANK2 gene. DNA Labs UAE offers a comprehensive genetic test for this condition, aimed at individuals who exhibit symptoms or […]
Long QT Syndrome (LQTS) is a rare, inherited heart condition that can lead to serious or even life-threatening arrhythmias. Among the genetic variants that can cause LQTS, mutations in the KCNE1 gene are responsible for Long QT Syndrome Type 5 (LQT5). Understanding the symptoms and getting an accurate diagnosis is crucial for managing the condition […]
DNA Labs UAE is a leading provider of genomics services in the United Arab Emirates. Our comprehensive range of services includes DNA sequencing, gene expression analysis, and SNP genotyping. With state-of-the-art equipment and a dedicated team of scientists and technicians, we ensure high-quality, accurate, and reliable data.
